期刊
JOURNAL OF APPLIED TOXICOLOGY
卷 34, 期 11, 页码 1226-1234出版社
WILEY
DOI: 10.1002/jat.3065
关键词
Nanoparticles; nanosilver; silver nanoparticles; genotoxicity; HepG2 cells; Caco2 cells; micronucleus; flow cytometry
类别
Two widely used in vitro cell culture models, human liver HepG2 cells and human colon Caco2 cells, and flow cytometry techniques were evaluated as tools for rapid screening of potential genotoxicity of food-related nanosilver. Comparative genotoxic potential of 20nm silver was evaluated in HepG2 and Caco2 cell cultures by a flow cytometric-based in vitro micronucleus assay. The nanosilver, characterized by the dynamic light scattering, transmission electron microscopy and inductively coupled plasma-mass spectrometry analysis, showed no agglomeration of the silver nanoparticles. The inductively coupled plasma-mass spectrometry and transmission electron microscopy analysis demonstrated the uptake of 20nm silver by both cell types. The 20nm silver exposure of HepG2 cells increased the concentration-dependent micronucleus formation sevenfold at 10 mu gml(-1) concentration in attached cell conditions and 1.3-fold in cell suspension conditions compared to the vehicle controls. However, compared to the vehicle controls, the 20nm silver exposure of Caco2 cells increased the micronucleus formation 1.2-fold at a concentration of 10 mu gml(-1) both in the attached cell conditions as well as in the cell suspension conditions. Our results of flow cytometric in vitro micronucleus assay appear to suggest that the HepG2 cells are more susceptible to the nanosilver-induced micronucleus formation than the Caco2 cells compared to the vehicle controls. However, our results also suggest that the widely used in vitro models, HepG2 and Caco2 cells and the flow cytometric in vitro micronucleus assay are valuable tools for the rapid screening of genotoxic potential of nanosilver and deserve more careful evaluation. Published 2014. This article is a U.S. Government work and is in the public domain in the USA.
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